HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596478Generated: October 30, 2026
Potassium Carbonate → HCID 54119206, compound
https://huagongshe.com/reaction/1596478
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | Cyclopropanemethanol | HCID 75644 | — |
| Reactant | Tetrafluoro-m-phenylenediamine dihydrochloride | HCID 149026 | — |
| Reactant | HCID 22016979 | HCID 22016979 | — |
| Reactant | HCID 69843878 | HCID 69843878 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54119206 | HCID 54119206 | 29% |
Reaction Steps
A cooled solution of cyclopropanemethanol (1.8 g; 25 mmol) in THF (7 mL) was added to a stirred 0C dispersion of CDI (4.05 g; 25 mmol) in THF (15 mL), and the reaction mixture was stirred for 30 minutes. A fraction of this solution (3.75 mL; 4.35 mmol) was added to a dispersion of 4-[3-(3,7-diazabicyclo[3.3.1]non-3-yl)-2(S)-hydroxypropoxy)benzonitrile (2.25 g; 6.0 mmol; dihydrochloride salt; prepared from 3,7-diazabicyclo[3.3.1]nonane-3-carboxylic acid and 7-[(2S)-3-(4-cyanophenoxy)-2-hydroxypropyl]-1,1-dimethylethyl ester, analogously to the method described in Example G above) and K2CO3 (2.0 g; 14.5 mmol) in THF (10 mL). The reaction mixture was heated (85° C.) in a sealed steel vessel for 24 hours, was then concentrated, and the residue partitioned between DCM and water. The organic layer was collected, dried, concentrated and subjected to column chromatography (DCM:MeOH; 95:5) to give the title compound in a 29% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06291475B1 |
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| Source dataset | uspto-grants-2001_09 |
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| ORD ID | ord-a40108d2ec174c5f973227e457c9a15f |
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| Source note | uspto-grants-2001_09 |
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